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Research historical outbreak investigations and the full recall archive, with charts, trends, and advanced filters. Looking for what's happening right now instead? See current Health Alerts.

Recall totals

All FDA and USDA recalls in Public Health Trace, June 2012 to September 2026.

37,061
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,786
Class I recallsReasonable probability of serious health consequences
24,313
Class II recallsTemporary or medically reversible health consequences
2,876
Class III recallsNot likely to cause adverse health consequences

Quick insights

A snapshot of the most notable patterns across all recorded FDA and USDA recalls.

Most recalled product100 vegetarian Fenugreek Capsules 90 count, 600mg, packaged in 150cc Amber Glass Packer with White Polypropylene Cap. 53 recalls
Most common hazardLack of Assurance of Sterility 2,072 recalls
Newest recallhttps://www.fsis.usda.gov/recalls-alerts/el-eden-import-distributor-corp-recalls-ineligible-pork-cracklings-products-importedPublished September 9, 2026
Most affected stateHawaii 200 recalls mention this state

Download matching recalls as CSV

CSV exports include up to 5,000 matching rows (applying your current filters), not the full dataset if it's larger.

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Recalls announced by month (Year to date)

A chart of recalls grouped by month.

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Source: FDA and USDA public dataLast updated

Summary (Year to date)

  • 1,527 recalls have been announced year to date.
  • Aug 2026 was 24% lower than the previous complete period (Jul 2026: 240).
  • The highest complete period was Jun 2026 (297).
  • Sep 2026 is incomplete and not included in the figures above.
  • Complete data
  • Incomplete
Recalls by class

A bar chart of the total number of recalls in this dataset by recall class.

Recalls by class
ClassRecalls
Class II24,313
Class I9,786
Class III2,876
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,313
Class I9,786
Class III2,876
Not Yet Classified2

Showing 1,361–1,380 of 18,725 recalls

FDA Recall United States Terminated Historical recordClass I

Harris Teeter

Product
ZENSHI HANDCRAFTED SUSHI Chef Sampler A#4 (Chili, Rainbow, C…
Reason
Salmonella. The firm received cucumbers which were recalled due to possible Salmonella. The cucumbers were used to make Sushi.
Published
July 9, 2025
Distribution
Product was shipped to the following sta…

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FDA Recall United States Terminated Historical recordClass I

Harris Teeter

Product
ZENSHI HANDCRAFTED SUSHI Chef Sampler A#3 (Crunchy, Rainbow,…
Reason
Salmonella. The firm received cucumbers which were recalled due to possible Salmonella. The cucumbers were used to make Sushi.
Published
July 9, 2025
Distribution
Product was shipped to the following sta…

View recall →

FDA Recall United States Terminated Historical recordClass I

Harris Teeter

Product
ZENSHI HANDCRAFTED SUSHI Chef Sampler A#1 (Rainbow, Crunchy,…
Reason
Salmonella. The firm received cucumbers which were recalled due to possible Salmonella. The cucumbers were used to make Sushi.
Published
July 9, 2025
Distribution
Product was shipped to the following sta…

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FDA Recall United States Terminated Historical recordClass I

Harris Teeter

Product
ZENSHI HANDCRAFTED SUSHI California Salad Roll 10pc (Brown R…
Reason
Salmonella. The firm received cucumbers which were recalled due to possible Salmonella. The cucumbers were used to make Sushi.
Published
July 9, 2025
Distribution
Product was shipped to the following sta…

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FDA Recall United States Terminated Historical recordClass I

Harris Teeter

Product
ZENSHI HANDCRAFTED SUSHI California Salad Roll 10pc Net Wt.…
Reason
Salmonella. The firm received cucumbers which were recalled due to possible Salmonella. The cucumbers were used to make Sushi.
Published
July 9, 2025
Distribution
Product was shipped to the following sta…

View recall →

FDA Recall United States Terminated Historical recordClass I

Harris Teeter

Product
ZENSHI HANDCRAFTED SUSHI California Roll 10pc Net Wt. 7.1oz…
Reason
Salmonella. The firm received cucumbers which were recalled due to possible Salmonella. The cucumbers were used to make Sushi.
Published
July 9, 2025
Distribution
Product was shipped to the following sta…

View recall →

FDA Recall United States Terminated Historical recordClass I

Harris Teeter

Product
ZENSHI HANDCRAFTED SUSHI Avocado Salad Roll 2pc Net Wt. 7.1o…
Reason
Salmonella. The firm received cucumbers which were recalled due to possible Salmonella. The cucumbers were used to make Sushi.
Published
July 9, 2025
Distribution
Product was shipped to the following sta…

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FDA Recall United States Terminated Historical recordClass I

Harris Teeter

Product
ZENSHI HANDCRAFTED SUSHI Arroz Picante Roll - Imitation Crab…
Reason
Salmonella. The firm received cucumbers which were recalled due to possible Salmonella. The cucumbers were used to make Sushi.
Published
July 9, 2025
Distribution
Product was shipped to the following sta…

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FDA Recall Ongoing Historical recordClass II

Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution, 0.2%/0.5%, 15 mL, Rx Only, Sterile, Manufactured by: Apotex Inc., Toronto, Ontario, Canada, M9L 1T9, Manufactured for: Apotex Corp., Weston, FL 33326, NDC 60505-0589-3

by Apotex Corp.

Reason
Lack of Assurance of Sterility
Published
July 2, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Azelastine HCl Ophthalmic Solution, USP, 0.05%, 6 mL, Rx Only, Sterile, Mfg. by: Apotex Inc., Toronto, Ontario, Canada, M9L 1T9, Mfg. for: Apotex Corp., Weston, FL 33326, NDC 60505-0578-4

by Apotex Corp.

Reason
Lack of Assurance of Sterility
Published
July 2, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Ketorolac Tromethamine Ophthalmic Solution, 0.5%, 10 mL, Rx Only, Manufactured by: Apotex Inc., Toronto, Ontario, Canada, M9L 1T9, Manufactured for: Apotex Corp., Weston, FL 33326, NDC 60505-1003-2

by Apotex Corp.

Reason
Lack of Assurance of Sterility
Published
July 2, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

0.9% Sodium Chloride Injection USP, 500 mL, packaged in 500 mL excel containers and further packaged 24 per case, Rx only, B.Braun Medical Inc., Bethlehem, PA 18018-3524, USA, NDC 0264-7800-10.

by B BRAUN MEDICAL INC

Reason
Lack of assurance of sterility: pinholes, within the finger boxes used during Form Fill Seal process resulting in leaks.
Published
July 2, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

0.9% Sodium Chloride Injection, USP, Flexible Plastic Container, Rx Only Fresenius Medical Care North America, Waltham, MA 02451, 1-800-323-5188, NDC 49230-300-10

by Fresenius Medical Care Holdings, Inc.

Reason
Lack of Assurance of Sterility
Published
July 2, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

DOBUTamine Injection, USP, 250 mg/20 mL (12.5 mg/mL), 20 mL per Single-dose Vial, carton of 10 Fliptop Vials, Rx only, For Intravenous Use Only, Made in Italy, Distributed by Hospira, Inc., Lake Forest, IL 60045 USA. NDC Carton: 0409-2344-02; NDC Vial: 0409-2344-62

by Pfizer Inc.

Reason
Discoloration; discolored solution from cracked vials
Published
July 2, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Nicotinamide adenine dinucleotide (NAD+): 100mg/mL, pre-filled syringe, Thrive Health Solutions, 88 Inverness, Cir E, Suite A-204, Englewood, CO 80112

by Thrive Health and Wellness, LLC, dba Thrive Health Solutions (Colorado)

Reason
Lack of Assurance of Sterility
Published
July 2, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Tirzepatide/Cyanocobalamin Injectable, 30mg/1mg/mL (15mg/0.5mg/0.5mL), pre-filled syringe, Thrive Health Solutions, 88 Inverness, Cir E, Suite A-204, Englewood, CO 80112

by Thrive Health and Wellness, LLC, dba Thrive Health Solutions (Colorado)

Reason
Lack of Assurance of Sterility
Published
July 2, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Tirzepatide/Cyanocobalamin Injectable, 15mg/1mg/mL, pre-filled syringe, Thrive Health Solutions, 88 Inverness, Cir E, Suite A-204, Englewood, CO 80112

by Thrive Health and Wellness, LLC, dba Thrive Health Solutions (Colorado)

Reason
Lack of Assurance of Sterility
Published
July 2, 2025
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Tirzepatide Injections, 30mg/mL, pre-filled syringe, Thrive Health Solutions, 88 Inverness, Cir E, Suite A-204, Englewood, CO 80112

by Thrive Health and Wellness, LLC, dba Thrive Health Solutions (Colorado)

Reason
Lack of Assurance of Sterility
Published
July 2, 2025
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Tirzepatide Injections, 20mg/mL, pre-filled syringe, Thrive Health Solutions, 88 Inverness, Cir E, Suite A-204, Englewood, CO 80112

by Thrive Health and Wellness, LLC, dba Thrive Health Solutions (Colorado)

Reason
Lack of Assurance of Sterility
Published
July 2, 2025
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Tirzepatide Injections, 10mg/mL, pre-filled syringe, Thrive Health Solutions, 88 Inverness, Cir E, Suite A-204, Englewood, CO 80112

by Thrive Health and Wellness, LLC, dba Thrive Health Solutions (Colorado)

Reason
Lack of Assurance of Sterility
Published
July 2, 2025
Distribution
Nationwide

View recall →

Data last updated:

Recall records are summarized from official FDA and USDA sources. Notices may be updated, reclassified, terminated, or withdrawn. Always review the linked official notice for the most current instructions. Read the full medical disclaimer.